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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Long term disease burden post-transplantation: three decades of observations in 25 Hurler patients successfully treated with hematopoietic stem cell transplantation (HSCT)

Fig. 1

Age at various disease manifestation onsets and surgical interventions with respect to time of transplantation (HSCT) in 25 patients with Mucopolysaccharidosis I Hurler (MPSI-H). The median age at HSCT was 21 months of age. The horizonal frequency distributions of disease manifestation onset (darked shaded bars) and surgical interventions (lighter shaded bars) are adjusted with respect to age at transplantation, such that events to the left of HSCT reflect pre-HSCT and those to the right post-HSCT

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172